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rs62514919

From SNPedia

Orientationminus
Geno Mag Summary
(G;T) 3 Carrier of a phenylketonuria mutation
(T;T) 0 common in clinvar
Make rs62514919(C;C)
Make rs62514919(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position102855273
GenePAH
is asnp
is mentioned by
dbSNPrs62514919
ebirs62514919
HLIrs62514919
Exacrs62514919
Varsomers62514919
Maprs62514919
PheGenIrs62514919
hapmaprs62514919
1000 genomesrs62514919
hgdprs62514919
ensemblrs62514919
gopubmedrs62514919
geneviewrs62514919
scholarrs62514919
googlers62514919
pharmgkbrs62514919
gwascentralrs62514919
openSNPrs62514919
23andMers62514919
23andMe allrs62514919
SNP Nexus

SNPshotrs62514919
SNPdbers62514919
MSV3drs62514919
GWAS Ctlgrs62514919
Max Magnitude3
ClinVar
Risk rs62514919(C;C)
Alt rs62514919(C;C)
Reference rs62514919(T;T)
Significance Untested
Disease not provided
Variation info
Gene PAH
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.103249051A>G
CLNSRC
CLNACC RCV000088989.1,